These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

253 related articles for article (PubMed ID: 25922366)

  • 1. The impact of human copy number variation on gene expression.
    Gamazon ER; Stranger BE
    Brief Funct Genomics; 2015 Sep; 14(5):352-7. PubMed ID: 25922366
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Highly Specific Genome-Wide Association Study Integrated with Transcriptome Data Reveals the Contribution of Copy Number Variations to Specialized Metabolites in Arabidopsis thaliana Accessions.
    Shirai K; Matsuda F; Nakabayashi R; Okamoto M; Tanaka M; Fujimoto A; Shimizu M; Shinozaki K; Seki M; Saito K; Hanada K
    Mol Biol Evol; 2017 Dec; 34(12):3111-3122. PubMed ID: 28961930
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Copy number variations and stroke.
    Colaianni V; Mazzei R; Cavallaro S
    Neurol Sci; 2016 Dec; 37(12):1895-1904. PubMed ID: 27393281
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Detection of copy number variation using SNP genotyping.
    Cooper GM; Mefford HC
    Methods Mol Biol; 2011; 767():243-52. PubMed ID: 21822880
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Copy number variations and human genetic disease.
    Mikhail FM
    Curr Opin Pediatr; 2014 Dec; 26(6):646-52. PubMed ID: 25198053
    [TBL] [Abstract][Full Text] [Related]  

  • 6. CONAN: copy number variation analysis software for genome-wide association studies.
    Forer L; Schönherr S; Weissensteiner H; Haider F; Kluckner T; Gieger C; Wichmann HE; Specht G; Kronenberg F; Kloss-Brandstätter A
    BMC Bioinformatics; 2010 Jun; 11():318. PubMed ID: 20546565
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The clinical context of copy number variation in the human genome.
    Lee C; Scherer SW
    Expert Rev Mol Med; 2010 Mar; 12():e8. PubMed ID: 20211047
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New Genome-Wide Methods for Elucidation of Candidate Copy Number Variations (CNVs) Contributing to Alzheimer's Disease Heritability.
    Szigeti K
    Methods Mol Biol; 2016; 1303():315-26. PubMed ID: 26235076
    [TBL] [Abstract][Full Text] [Related]  

  • 9. An Evolutionary Perspective on the Impact of Genomic Copy Number Variation on Human Health.
    Saitou M; Gokcumen O
    J Mol Evol; 2020 Jan; 88(1):104-119. PubMed ID: 31522275
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Structural architecture of SNP effects on complex traits.
    Gamazon ER; Cox NJ; Davis LK
    Am J Hum Genet; 2014 Nov; 95(5):477-89. PubMed ID: 25307299
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Progress from genome-wide association studies and copy number variant studies in epilepsy.
    Leu C; Coppola A; Sisodiya SM
    Curr Opin Neurol; 2016 Apr; 29(2):158-67. PubMed ID: 26886358
    [TBL] [Abstract][Full Text] [Related]  

  • 12. CNVs of noncoding cis-regulatory elements in human disease.
    Spielmann M; Klopocki E
    Curr Opin Genet Dev; 2013 Jun; 23(3):249-56. PubMed ID: 23601627
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?
    Hosak L; Silhan P; Hosakova J
    Neuro Endocrinol Lett; 2012; 33(2):183-90. PubMed ID: 22592199
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The impact of human copy number variation on a new era of genetic testing.
    Choy KW; Setlur SR; Lee C; Lau TK
    BJOG; 2010 Mar; 117(4):391-8. PubMed ID: 20105165
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Implications of gene copy-number variation in health and diseases.
    Almal SH; Padh H
    J Hum Genet; 2012 Jan; 57(1):6-13. PubMed ID: 21956041
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Relating CNVs to transcriptome data at fine resolution: assessment of the effect of variant size, type, and overlap with functional regions.
    Schlattl A; Anders S; Waszak SM; Huber W; Korbel JO
    Genome Res; 2011 Dec; 21(12):2004-13. PubMed ID: 21862627
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [DNA polymorphisms].
    Suehiro Y; Furuya T; Sasaki K; Hinota Y
    Rinsho Byori; 2013 Nov; 61(11):1001-7. PubMed ID: 24450105
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical interpretation of copy number variants in the human genome.
    Nowakowska B
    J Appl Genet; 2017 Nov; 58(4):449-457. PubMed ID: 28963714
    [TBL] [Abstract][Full Text] [Related]  

  • 19. New technologies provide insights into genetic basis of psychiatric disorders and explain their co-morbidity.
    Rudan I
    Psychiatr Danub; 2010 Jun; 22(2):190-2. PubMed ID: 20562745
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Characterization of copy number-stable regions in the human genome.
    Johansson AC; Feuk L
    Hum Mutat; 2011 Aug; 32(8):947-55. PubMed ID: 21542059
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.